Search results for " Biochemicals"
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				Upstream Processing: Biochemicals and Raw Materials
								
	 
	
	
	
		Experts reveal how to identify the “right” biochemical, the process of sourcing biochemicals, sourcing challenges, and what industry professionals should know about the space.  
		
	
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				Preclinical Evaluation of Product Related Impurities and Variants
								Preclinical Evaluation of Product Related Impurities and Variants
	The approaches for sample preparation of preclinical evaluation of safety and efficacy are addressed taking into consideration the s…								
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				Tools for Continuous Bioprocessing Development
								
	Could perfusion microbioreactors bring more agility to biomanufacturing?
	
	By Rajeev J. Ram
	In semiconductor manufacturing, for example, a thorough understanding of process variation allows co…								
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				Fermentation for the Future
								
	Improving efficiency, value chain, quality, and protein complexity with advanced bioprocess development. 
	Jan 01, 2015 
	
	By Cynthia Challener, PhD 
	
	Microorganisms—bacteria and yeast—have b…								
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				Leveraging Computational Models of Glycosylation for Biopharma QA
								
	Close collaboration between academic and industrial groups is vital to ensuring glycosylation models are fit for deployment. 
	
	  
	
	
	By Ioscani Jiménez del Val 
	
	
	  
	 
	
	  Good Studio/S…								
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				Real-Time Characterization of Biotherapeutics and Comparability of Biosimilars
								Real-Time Characterization of Biotherapeutics and Comparability of Biosimilars
	A major advantage of SPR-based analysis is its ability to estimate the association and dissociation rate constants, an …								
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				Techniques for Improving Process Development for Exosome-Derived Therapeutics
								
	An interview with Aaron Noyes, Head of Downstream Processing at Codiak BioSciences 
	
	
	
	
	
	Some therapeutic targets have long frustrated drug developers hoping to crack the code of mitigating un…								
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				Being Thorough When Transferring Technology
								
	Communication and taking the time to develop the process are key to successful transfer and scale up of biologics. 
	By Susan Haigney 
	Editor's note: The following is an extended version of the…								
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				Downstream Processing for Cell-Based Therapies
								
	By Qasim A. Rafiq, Fernanda Masri 
	With increasing numbers of advanced therapies—including cell and gene therapies—entering early- and late-stage clinical development, significant focus has been …								
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				Impact of Manufacturing-Scale Freeze-Thaw Conditions on a mAb Solution
								
	The objective of this study was to assess the impact of manufacturing-scale, freeze-thaw conditions on aggregation and subvisible particle formation of a monoclonal antibody solution (mAb-A; IgG1) u…